Interferon-gamma acts directly on rejecting renal allografts to prevent graft necrosis

In transplant rejection interferon (IFN)-gamma regulates the recipient immu ne response but also acts directly on IFN-gamma receptors in the graft. We investigated these direct actions by comparing rejecting kidneys from donor s lacking IFN-gamma receptors (GRKO mice) or control donors (129Sv/J) in CB A recipients, Beginning day 5, 129Sv/J kidneys displayed high major histoco mpatibility complex (MHC) expression, progressive infiltration by inflammat ory cells, but no thrombosis and little necrosis, even at day 21, GRKO kidn eys showed increasing fibrin thrombi in small veins, peritubular capillary congestion, hyaline casts, and patchy parenchymal necrosis, progressing to near total necrosis at day 10. Terminal dUTP nick-end labeling assays were positive only in the interstitial infiltrate, confirming that massive cell death in GRKO transplants was not apoptotic. Paradoxically, GRKO kidneys sh owed little donor MHC induction and less inflammatory infiltration. Both GR KO and 129Sv/J allografts evoked vigorous host immune responses including a lloantibody and mRNA for cytotoxic T cell genes (perforin, granzyme B, Fas ligand), and displayed similar expression of complement inhibitors (CD46, C D55, CD59). GRKO kidneys displayed less mRNA for inducible nitric oxide syn thase and monokine inducible by IFN-gamma but increased heme oxygenase-l mR NA. Thus IFN-gamma acting on IFN-gamma receptors in allografts promotes inf iltration and MHC induction but prevents early thrombosis, congestion, and necrosis.